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up and up 12 hour cough relief

NDC 11673-114 · Target Corporation

Generic namedextromethorphan polistirex
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE
Strength30 mg/5mL
Pharmacologic classSigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

11673-114-28 — 1 BOTTLE in 1 CARTON (11673-114-28) / 148 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0904-7513 — Guaifenesin and Dextromethorphan, 0904-7531 — brompheniramine maleate, dextromethorphan hydrobromide, 0924-0142 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 10202-740 — Dextromethorphan HBr, Guaifenesin, 10956-846 — Dextromethorphan Hydrobromide / Guaifenesin, 11383-311 — Dextromethorphan HBr, Guaifenesin, 11523-0008 — chlorpheniramine maleate, dextromethorphan hydrochloride, 11523-0038 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, 11523-4326 — Chlorpheniramine maleate and Dextromethorphan hydrobromide, 11523-4358 — Acetaminophen,Dextromethorphan hydrobromide, doxylamine succinate, 11673-267 — Guaifenesin and Dextromethorphan HBr, 11673-287 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 11673-312 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 11673-322 — Acetaminophen, Dextromethrophan, Doxylamine succinate, Phenylephrine HCl, 11673-337 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 11673-347 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 11673-410 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-627 — Dextromethorphan HBr, Guaifenesin, 11673-698 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 11673-716 — dextromethorphan hydrobromide, guaifenesin, +1967 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.